Associate Clinical Project Manager, Sponsor Dedicated

This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up through database lock and closeout. The role ensures high-quality data delivery and regulatory compliance across all phases of the trial, collaborating closely with cross-functional teams.

Requirements

• Three years of clinical trial management experience is required within a role that is accountable for driving and owning local trial activites at the regional level.
• Bachelor's Degree In life sciences or related field required
• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.

Benefits

• Medical, dental, vision, and life insurance
• Retirement savings plans (401(k), etc.)
• Paid time off (vacation, sick leave, etc.)